pERT84-10-质粒载体-ATCC-DSM-CCUG-泰斯拓生物

你好,请登录   免费注册    |    收藏本站
联系电话: 0574-87917803
联系电话: 0574-87917803
pERT84-10
pERT84-10
规格:
货期:
编号:TS134191
品牌:Testobio
产品名称: pERT84-10
商品货号: TS134191
Designations: pERT84-10
Species: Homo sapiens, human
Depositors: LM Kunkel
Vector:
Construct size (kb): 6.900000095367432
Insert:
DNA: genomic
Insert lengths(kb): 2.5
Gene product: DNA Segment, single copy (within DMD gene) DXS142
Alleles: A1, A2
Insert Size (kb): 2.5
Media: ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Shipping Information: Distributed: freeze-dried
Comments:
Restriction digests of the clone give the following sizes (kb): HindIII--4.4, 1.8, 0.8; EcoRI--6.9; PstI--6.9; BamHI--4.4, 2.5; SalI--6.9.
This clone is at the 5 most end of the DMD locus.
HindIII digestion yields 2 fragments from the insert: 1.8 kb and 0.7 kb. The larger fragment recognizes the two constant TaqI bands of 3.4 and 1.75 kb. The 0.7 kb HindIII fragment detects the TaqI RFLP.
The polymorphisms detected by this probe are contained within the DMD locus.
References:

Koenig M, et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50: 509-517, 1987. PubMed: 3607877

Bertelson CJ, et al. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. J. Med. Genet. 23: 531-537, 1986. PubMed: 2879924

Kunkel LM, et al. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc. Natl. Acad. Sci. USA 82: 4778-4782, 1985. PubMed: 2991893

Louis M Kunkel, personal communication

首页 > 产品中心 > 微生物培养 > 菌株 > null > pERT84-10

pERT84-10

  • 货号: TS134191
  • 好评
有货
  • 品牌 : TESTOBIO
产品名称: pERT84-10
商品货号: TS134191
Designations: pERT84-10
Species: Homo sapiens, human
Depositors: LM Kunkel
Vector:
Construct size (kb): 6.900000095367432
Insert:
DNA: genomic
Insert lengths(kb): 2.5
Gene product: DNA Segment, single copy (within DMD gene) DXS142
Alleles: A1, A2
Insert Size (kb): 2.5
Media: ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin
Biosafety Level: 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Shipping Information: Distributed: freeze-dried
Comments:
Restriction digests of the clone give the following sizes (kb): HindIII--4.4, 1.8, 0.8; EcoRI--6.9; PstI--6.9; BamHI--4.4, 2.5; SalI--6.9.
This clone is at the 5 most end of the DMD locus.
HindIII digestion yields 2 fragments from the insert: 1.8 kb and 0.7 kb. The larger fragment recognizes the two constant TaqI bands of 3.4 and 1.75 kb. The 0.7 kb HindIII fragment detects the TaqI RFLP.
The polymorphisms detected by this probe are contained within the DMD locus.
References:

Koenig M, et al. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. Cell 50: 509-517, 1987. PubMed: 3607877

Bertelson CJ, et al. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. J. Med. Genet. 23: 531-537, 1986. PubMed: 2879924

Kunkel LM, et al. Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. Proc. Natl. Acad. Sci. USA 82: 4778-4782, 1985. PubMed: 2991893

Louis M Kunkel, personal communication

合作单位: